Chowdhury, M.R. and Moshikur, R.M. and Wakabayashi, R. and Tahara, Y. and Kamiya, N. and Moniruzzaman, M. and Goto, M. (2018) Ionic-Liquid-Based Paclitaxel Preparation: A New Potential Formulation for Cancer Treatment. Molecular Pharmaceutics, 15 (6). pp. 2484-2488.
Full text not available from this repository.Abstract
Paclitaxel (PTX) injection (i.e., Taxol) has been used as an effective chemotherapeutic treatment for various cancers. However, the current Taxol formulation contains Cremophor EL, which causes hypersensitivity reactions during intravenous administration and precipitation by aqueous dilution. This communication reports the preliminary results on the ionic liquid (IL)-based PTX formulations developed to address the aforementioned issues. The formulations were composed of PTX/cholinium amino acid ILs/ethanol/Tween-80/water. A significant enhancement in the solubility of PTX was observed with considerable correlation with the density and viscosity of the ILs, and with the side chain of the amino acids used as anions in the ILs. Moreover, the formulations were stable for up to 3 months. The driving force for the stability of the formulation was hypothesized to be the involvement of different types of interactions between the IL and PTX. In vitro cytotoxicity and antitumor activity of the IL-based formulations were evaluated on HeLa cells. The IL vehicles without PTX were found to be less cytotoxic than Taxol, while both the IL-based PTX formulation and Taxol exhibited similar antitumor activity. Finally, in vitro hypersensitivity reactions were evaluated on THP-1 cells and found to be significantly lower with the IL-based formulation than Taxol. This study demonstrated that specially designed ILs could provide a potentially safer alternative to Cremophor EL as an effective PTX formulation for cancer treatment giving fewer hypersensitivity reactions. © 2018 American Chemical Society.
Item Type: | Article |
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Impact Factor: | cited By 0 |
Uncontrolled Keywords: | CD86 antigen; cell surface marker; cremophor; intercellular adhesion molecule 1; ionic liquid; paclitaxel, allergic reaction; antigen expression; antineoplastic activity; Article; complex formation; controlled study; cytotoxicity; drug formulation; drug megadose; drug solubility; drug stability; female; HeLa cell line; human; human cell; in vitro study; preliminary data; priority journal; THP-1 cell line |
Depositing User: | Mr Ahmad Suhairi Mohamed Lazim |
Date Deposited: | 26 Feb 2019 02:32 |
Last Modified: | 26 Feb 2019 02:32 |
URI: | http://scholars.utp.edu.my/id/eprint/20856 |